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170results about How to "Reduce the rate of hydrolysis" patented technology

Method for preparing uvioresistant polyester by nanometer titania generated in situ

A process for in-situ preparing UV-resistant polyester by use of TiO2 nanoparticles includes such steps as synthesizing the hydrolysis speed controllable glycol salt of Ti, organic stabilizing it, dispersing it in diol, and polymerizing (or copolymerizing) with polyester and other monomers. Its advantage is high UV shielding effect.
Owner:SHANGHAI JIAO TONG UNIV

Health care composition capable of reducing blood sugar, medicinal granules and preparation method of medicinal granules

The invention discloses a health care composition capable of reducing blood sugar, medicinal granules and a preparation method of the medicinal granules, and belongs to the technical field of food processing. The health care composition capable of reducing blood sugar consists of the following components in parts by weight: 8-15 parts of oat flour, 3-6 parts of tartary buckwheat powder, 2-5 parts of long-chain inulin, 2-4 parts of L-arabinose, 1-4 parts of milk powder, 1-5 parts of a navy bean extract, 0.5-1.5 parts of konjaku flour and 0.005-0.02 part of sucralose. The health care composition has the efficacy of reducing the postprandial blood sugar level of people suffering from hyperglycemia in an auxiliary manner, and can effectively prevent the postprandial blood sugar value from quickly rising, wherein the oat flour, the tartary buckwheat powder, the long-chain inulin, the L-arabinose, the navy bean extract and the konjaku flour have mutual synergistic effects and multiplicative effects in the respect of reducing the blood sugar, can reduce the postprandial blood sugar level of diabetes patients through a plurality of respects, and can reduce the damage of high blood sugar to bodies.
Owner:HENAN UNIV OF SCI & TECH

Collosol gel production method of nano NiO material

A process for preparing NiO nanoparticles in the form of tetragonal crystal by sol-gel method includes dissolving polyethanediol in deionized water, adding less ammonia water to regulate pH=7.5-8, dissolving nickel acetate in absolute alcohol, slowly adding the solution to said aqueous solution of polyethanediol, high-speed stirring, holding temp at 70 deg.c for 4 hr while stirring to obtain sol, filtering, drying and calcining at 500 deg.C for 2 hr.
Owner:SHANGHAI UNIV

Preparation method for plant oil-based polyurethane coated fertilizer having improved water resistance

The invention discloses a preparation method for plant oil-based polyurethane coated fertilizer having improved water resistance. The preparation method comprises the following steps that step 1, modification treatment is performed on plant oil polyalcohol, wherein by weight, 0.2%-5% of hydrolysis stabilizer is added into the plant oil polyalcohol and stirred at high temperature, so that modified plant oil polyalcohol is obtained; step 2, The polyurethane coated urea slow-release fertilizer is prepared, wherein large-particle urea is taken by weighing, the temperature is raised to 78-80 DEG C and is maintained, the modified plant oil polyalcohol prepared in the step 1 and lubricant are fully mixed and fused through a coating method, afterwards, the mixture and liquid isocyanate resin are quickly mixed, the surfaces of urea particles are evenly coated with the mixture, the urea particles and the coating liquid are fully mixed in a revolving drum, the coating liquid is gradually subjected to crosslinking solidification, and finally the polyurethane coated urea slow-release fertilizer is formed. Water resistance testing is performed on the prepared plant oil-based polyurethane coated urea, and a good result is obtained.
Owner:中国-阿拉伯化肥有限公司

Isophthalonitrile dehydration hydrogenation method

InactiveCN101062899AReduce the rate of condensation polymer formation andExtended service lifeCatalyst carriersOrganic compound preparationChemistryFixed bed
The invention discloses a method of isophthalonitrile dehydration and hydrogenation, which comprises the following steps: stripping moisture in the fixed bed with molecular dewatering screen under room temperature ; setting the air speed of dehydration at 2-5h-1; proceeding hydrogenation under the function of activator; proceeding hydrogenation in two series tubular reactor. This invention decreases the generating speed of polycondensation and dewatering speed of middle product of hydrogenation, which can prolong durability of activator.
Owner:上海博润石化科技发展有限公司

Ultrafine coated cadmium selenide sulfide ceramic pigment and preparation method thereof

The invention discloses an ultrafine coated cadmium selenide sulfide ceramic pigment preparation method, which comprises: (1) dissolving a cadmium salt and a surfactant into water to obtain a solutionA, dissolving sodium sulfide and selenium into water to obtain an alkaline solution, adding the solution A into the alkaline solution in a dropwise manner to obtain a cadmium selenide sulfide precursor, and carrying out a hydrothermal reaction to obtain dispersed cadmium selenide sulfide; 2) adding a water glass solution into an acid solution, and controlling the pH value to obtain a silicic acidsolution; 3) adding the dispersed cadmium selenide sulfide into a zirconium oxychloride dispersion liquid, adding the silicic acid solution, adjusting the concentrations of the silicon ions and the zirconium ions, adjusting the pH value, and heating to obtain a gel; and 4) drying the gel, uniformly mixing the dried gel and a mineralizing agent, and calcining to obtain the ultrafine coated cadmiumselenide sulfide ceramic pigment. According to the invention, the particle size D100 of the pigment prepared by the method is less than 1.3 [mu]m, and the method has good condition controllability and good reproducibility, and is suitable for large-scale production.
Owner:GUANGDONG DOWSTONE TECH

Preparation method of low temperature liquid phase precipitation process bismuth oxyiodide visible light photocatalyst

The invention relates to a preparation method of a low temperature liquid phase precipitation process bismuth oxyiodide visible light photocatalyst. Organic acid assisted regulation and low temperature liquid phase precipitation process are employed to prepare the bismuth oxyiodide photocatalyst, the coordinating complexation of organic acid and bismuth ions is utilized to reduce the hydrolysis rate of bismuth ions and regulate the growth rate, structure and morphology of bismuth oxyiodide crystal nucleus, and white light LED is adopted as the simulated visible light source for photocatalyticdegradation of the dye solution. The preparation method of the bismuth oxyiodide photocatalyst provided by the invention has the characteristics of simple and feasible operation, no need for adding ofmacromolecule or surfactant, reaction under low temperature or room temperature condition, low energy consumption and short reaction time. After 80-100min irradiation by white light LED, the photocatalytic degradation of the bismuth oxyiodide photocatalyst on a dye solution almost achieves equilibrium, and after 100min irradiation by white light LED, the photocatalytic dye degradation efficiencyof the bismuth oxyiodide photocatalyst on 10mg / L and 50mg / L dye solutions respectively reach 75-96% and 35-46%, and after five cycles of utilization, the photocatalytic dye degradation rate of the bismuth oxyiodide photocatalyst is 70-85% of the first photocatalytic dye degradation rate, therefore the bismuth oxyiodide photocatalyst can be widely applied in visible light photocatalytic degradation, dye wastewater pollution treatment and other fields.
Owner:CHENGDU UNIVERSITY OF TECHNOLOGY

Preparation method for novel negative electrode material of lithium ion battery

The invention relates to a preparation method for a novel negative electrode material of a lithium ion battery, belongs to the technical field of a lithium ion battery material, and aims to provide a preparation method for a novel nanometer SnO<2> / C composite negative electrode material of the lithium ion battery. The preparation method for the novel negative electrode material of the lithium ion battery comprises the steps of dissolving a tin source into a mixed acetone water system, stirring until the tin source is fully dissolved, then adding urea and polyvinylpyrrolidone, stirring for 2-5h, then adding expanded graphite, next, moving the solution to a hydrothermal reaction kettle, and performing hydrothermal synthesis at a temperature of 90-130 DEG C for 2-10h, naturally cooling the reaction kettle to the room temperature, and performing suction filtration, washing and drying on the obtained product, and baking under an inert atmosphere at a temperature of 600 DEG C for 3h to obtain the nanometer SnO<2> / C composite negative electrode material of the lithium ion battery.
Owner:SHANXI UNIV

Preparation method of lithium-ion battery negative electrode molybdenum disulfide and application thereof

The invention discloses a preparation method of lithium-ion battery negative electrode molybdenum disulfide and the application thereof. The preparation method comprises the following steps: mixing sodium molybdate dehydrate, thiourea, water and diethylene glycol to carry out a hydrothermal reaction, separating the product after the hydrothermal reaction, performing calcination treatment on the separated solids in argon-hydrogen mixed gas, and finally cooling to a room temperature, so as to obtain the lithium-ion battery negative electrode material molybdenum disulfide. According to the preparation method disclosed by the invention, the hydrolysis rate of the thiourea is reduced by adding the diethylene glycol, so that the aim of controlling the reaction rate of sodium molybdate is achieved. Two-dimensional molybdenum disulfide nanosheets are assembled into a three-dimensional layered flower structure, so that the specific advantages of the molybdenum disulfide can be preserved, the condition that the molybdenum disulfide is irreversibly overlapped can be avoided, and a larger contact area is provided.
Owner:JIANGHAN UNIVERSITY

Preparation method for hollow titanium dioxide/polyacrylate composite film with insulation performance

The invention relates to a preparation method for a hollow titanium dioxide / polyacrylate composite film with an insulation performance. A template method for preparing hollow titanium dioxide needs to be finished by two steps, and the process is complex. The preparation method disclosed by the invention comprises the following steps: dispersing polystyrene microspheres in absolute ethyl alcohol and ultrasonically treating to form mixed solution A; adding butyl titanate in absolute ethyl alcohol to form mixed solution B; dripping the mixed solution B and ammonia water into the mixed solution A; heating and stirring in a water bath to obtain a white turbid liquid, carrying out a centrifugal treatment, washing and drying to obtain hollow titanium dioxide particles, ultrasonically dispersing the hollow titanium dioxide particles in distilled water, and mixing and stirring with a polyacrylate emulsion to obtain a composite emulsion; then taking the composite emulsion in a polytetrafluoroethylene plate and carrying out film formation to obtain the hollow titanium dioxide / polyacrylate composite film. The preparation method disclosed by the invention realizes one-step synthesis for hollow titanium dioxide with a regular structure, and overcomes the defect of a complex process; moreover, the hydrolysis speed of butyl titanate is reduced through the ammonia water, the uniform coating of titanium dioxide is realized, and hollow titanium dioxide with the regular structure is formed.
Owner:SHAANXI UNIV OF SCI & TECH

Preparation method of adsorbent containing SnO2/Sb2O5, product and application of adsorbent

The invention relates to a preparation method of an adsorbent containing SnO2/Sb2O5. According to the method, SbCl3 with a stable chemical property and low toxicity is taken as a Sb source, sodium thiosulfate pentahydrate, namely SnCl4, is utilized as a Sn source, and a SnO2/Sb2O5 binary composite oxide is prepared. The preparation method comprises the following steps of oxidizing Sb<3+> as Sb(V) in a non-water system taking alcohol as a solvent by adopting the combination of H2O2 oxidation and ultraviolet irradiation, further carrying out hydrolytic precipitation on Sb(V) and Sb<4+> by utilizing a small amount of water introduced by utilizing H2O2 solution as a reactant, and forming a binary SnO2/Sb2O5 composite oxide. The method provided by the invention has the advantages that the hydrolyzing speed of Sb<3+> is slow, the generation of the Sb2O3 is effectively controlled, the Sn/Sb2O5 binary composite oxide with the Sb<3+> oxygenation efficiency being 100% is obtained, the adsorbent can remove the radioactive isotope Co ions and a complex thereof and stable isotope Co ions and a complex thereof, and the adsorptive property of the SnO2/Sb2O5 binary composite oxide and pure Sb2O5 obtained by the introduction of Sb is improved by 200 times.
Owner:TSINGHUA UNIV

Alkyl polyoxyether and preparation method thereof, and polycarboxylate superplasticizer prepared from alkyl polyoxyether and preparation method thereof

ActiveCN106916292APromote adsorptionGood slump retentionWater reducerSuperplasticizer
The invention provides alkyl polyoxyether with a structure as shown in a formula (I) or formula (II) which is described in the specification. The invention also provides a preparation method for the alkyl polyoxyether, a polycarboxylate superplasticizer prepared with the alkyl polyoxyether as a polymerization monomer and a preparation method for the polycarboxylate superplasticizer. The alkyl polyoxyether provided by the invention contains a phenyl ring which exerts great steric hindrance effect in a polymer molecule in preparation of the polycarboxylate superplasticizer, so the prepared polycarboxylate superplasticizer is endowed with better slump loss resistance. The polycarboxylate superplasticizer provided by the invention uses the alkyl polyoxyether as the monomer, has the both advantages of high water-reducing rate and high slump loss resistance, and is convenient to use and obviously reduced in the doping rate in concrete; so cost for production and construction is reduced, requirements of environmental protection are better met, and immense economic and social benefits can be produced.
Owner:JIANGSU OXIRANCHEM CO LTD

Preparation method and application of graphene/lithium titanate composite material

The invention provides a preparation method and application of a graphene/lithium titanate composite material. The preparation method comprises the following steps: preparing a titanium source dispersion liquid from tetrabutyl titanate, graphene, P123 and tert-butyl alcohol, and preparing a lithium source solution from lithium acetate dihydrate, deionized water and tert-butyl alcohol; transferring the titanium source dispersion liquid to a microwave reactor and heating the titanium source dispersion liquid till reflux, adding the lithium source solution to react for a certain time, cooling the reactant, removing a solvent and then drying the product, thus obtaining a graphene-based lithium titanate precursor; placing the obtained graphene-based lithium titanate precursor in a tube furnace to be calcined at a certain temperature for a certain time under the protection of an inert gas, thus obtaining the graphene/lithium titanate composite material. The obtained active material, acetylene black and PVDF (polyvinylidene fluoride) are mixed uniformly to coat an aluminium foil to prepare an electrode slice of a button cell, finally a half cell is assembled in a glove box, charge and discharge performances are tested, the half cell is made from the active material and the performances are detected. Through detection, the capacity of graphene/lithium titanate under the condition of 1C rate is still 140mAh/g, can still keep more than 99% of capacity after circulation for 1000 times, and has excellent performances.
Owner:江苏江大环保科技开发有限公司

A Stannic Oxide Microballoon with Controllable Crystallite Dimension and its Preparation Method and Application

This invention involves a kind of stannic oxide microballoon with controllable crystallite dimension and its preparation method and application. This stannic oxide microballoon is composed of stannic oxide microcrystal with fine crystallinity through self-assembly. The grain size of stannic oxide microcrystal is adjustable within range of 5-30nm. The diameter of stannic oxide microballoon is 200-400nm and its specific surface area >40m2 / g; During preparation, add concentrated hydrochloric acid and tin source into the mixed solution of normal propyl alcohol and water in order, forming the transparent homogeneous solution; Conduct solvothermal reaction; After the reaction ends, take out the sediment, wash and separate it. Being compared with the current technology, this invention has simple and easy process route, which does not need surface active agent. And the multilevel structure Sno2 microballoon with equally distributed dimension can be gotten through one-step method, which is composed of stannic oxide microcrystal through self-assembly. Also, the dimension of Sno2 microcrystal can be adjusted and controlled through adjusting the alcohol / water proportion in the reaction system. The microballoon has features of high specific area and submicron level dimension, which has wide application prospect in areas of solar cell, lithium ion battery and photocatalysis.
Owner:SHANGHAI UNIV OF ENG SCI
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